Canonical Allele Identifier: PA2825410753
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1951228
ClinVar RCV Id: RCV002685996
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035963.1:p.Arg314Cys
CA10406084
NM_001042498.3:c.940C>T